Clinical Research Associate II

Psi CRO; Çankaya; Hybrid; TRY 150,000 - 210,000; Full time

Job summary

Psi CRO in Ankara, Turkey is seeking a Clinical Research Associate II to oversee monitoring visits, ensure data quality, and maintain site relationships across therapeutic indications. The role emphasizes patient safety, regulatory compliance, and timely study delivery.

You should have a Life Sciences degree, 2–3 years on-site monitoring experience in Phase II/III, Turkish native with English at least B2, proficiency in MS Office, and willingness to travel between sites.

Qualifications

• Degree in Life Sciences or equivalent.
• 2–3 years of independent on-site monitoring experience.
• Experience in Phase II and/or III monitoring visits.
• Native Turkish and English (B2).
• Willingness to travel between sites.

Responsibilities

• Prepare, conduct, and report monitoring visits.
• Support quality control and reports review.
• Coordinate with clinical investigators, vendors and staff.
• Handle Investigational Product and trial supplies at sites.
• Provide training to investigators and site staff.
• Assist with site identification and feasibility research.
• Support Regulatory Affairs in site regulatory documents.
• Present at Investigator's Meetings.
• Maintain study tracking systems.
• Assist audits and resolve findings.

Skills

On-site monitoring

Site coordination

Data quality

MS Office

Travel

Communication

Education

Bachelor in Life Sciences

Tools

MS Office

Job description

We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 3000 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.

Job Description

As a Clinical Research Associate II,you will work on the frontline of communication with project stakeholders, ensuring timelines, targets, and standards of clinical research projects in a variety of therapeutic indications. You will build and maintain relationships with clinical sites and investigators. You will focus on subjects' rights, safety and well-being and quality of data compliance.

Hybrid role in Ankara, Turkey

Your responsibilities will include:

• Preparation, conduct, and reporting of all types of monitoring visits
• Supporting quality control, such as compliance monitoring and reports review
• Contact for clinical investigators, vendors and support services in regard to study progress
• Proper handling, use, accountability, reconciliation, and return of all Investigational Product(s) and trial supplies at sites
• Delivering training of investigators, site staff and project teams
• Be involved in site identification process and feasibility research
• Support to Regulatory Affairs in procurement of site regulatory documents
• Preparation and delivering of presentations at Investigator's Meetings
• Maintenance of study-specific automated tracking systems
• Preparation for and attendance at company's audits; resolution of audit findings

Qualifications

• Degree in Life Sciences (or similar), or an equivalent combination of education, training & experience
• 2-3 years of independent on-site monitoring experience
• Experience in all types of monitoring visits in Phase II and/or III
• Native Turkish and full working proficiency in English (B2)
• Experience supporting Oncology studies is beneficial, but not essential
• Proficiency in MS Office applications
• Ability to plan, multitask and work in a dynamic team environment
• Communication, collaboration, and problem-solving skills
• As you will be monitoring multiple sites, you must have a valid driver's license, and the ability to travel.

Additional Information

This is a great opportunity for you to further develop your skills, widen your therapeutic area experience, and become an expert in clinical research.